4.7 Article

Pyrolysis synthesis of CuWO4@C composite catalysts as Pt-free counter electrode for dye-sensitized solar cells

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DOI: 10.1016/j.jaap.2023.105873

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Pyrolysis; Polyoxotungstate; Polyaniline; Dye -sensitized solar cells; Counter electrode

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Transition metal compound catalysts have potential applications in Pt-free counter electrodes (CEs) for reducing costs and improving power conversion efficiency (PCE) of dye-sensitized solar cells (DSSCs). In this study, CuWO4@C composite catalysts were synthesized by pyrolyzing Cu-based polyoxotungstate (H3PW12O40) precursor in the presence of polyaniline. The effects of pyrolysis temperature on the composition, morphology, and structure of the CuWO4@C composite were investigated. The optimal pyrolysis temperature of 800 degrees C resulted in the highest PCE of 7.11% for the regeneration of I3/I couple in the DSSCs.
Transition metal compound catalysts have potential applications in Pt-free counter electrode (CE), which are one of the important strategies for reducing costs and improving power conversion efficiency (PCE) of dye-sensitized solar cells (DSSCs). Herein, CuWO4@C composite catalysts were synthesized by pyrolyzing Cu-based polyoxotungstate (H3PW12O40) precursor in presence of polyaniline. The effect of pyrolysis temperature (600, 700, 800, 900, 1000 and 1100 degrees C) on the compositions, morphologies and structures of CuWO4@C composite was investigated by Thermogravimetry-Derivative thermogravimetry-Differential scanning calorimetry (TG-DTGDSC) simultaneous, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Scanning electron microscopy (SEM) and N2 adsorption-desorption analysis. The photovoltaic properties of different CuWO4@C composites CEs were determined by photocurrent-photovoltage (J-V) measurement. The results reveal that the pyrolysis at 800 degrees C was optimum to get the best CuWO4@C composite CE, which yielded the highest PCE of 7.11% for the regeneration of I3 /I couple in the DSSCs. The structure-activity relationship of the CuWO4@C composite catalysts was discussed.

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